Clinical Research ociate Shaghai China
Clinical Research ociate Shaghai China
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Salary Not Disclosed
1 Vacancy
Job Description
- Manage daily clinical trial operations and ensure compliance with study protocols.
- Review clinical trial protocols and participate in the design and of clinical studies.
- Collaborate with clinical operations teams providing support throughout the trial lifecycle.
- Conduct site monitoring as required following instructions from the Project Manager (likely once or twice monthly).
- Perform data analysis interpret results and contribute to research efforts.
- Liaise with the medical and scientific community to provide necessary trial support.
- Bachelor s or Master s degree in a related scientific field.
- 25 years of experience as a Clinical Research Associate.
- Strong knowledge and handson experience in clinical trials and monitoring.
- Proven ability to create review and implement clinical trial protocols.
- Experience in clinical operations including site management monitoring and data management.
- Familiarity with Good Clinical Practice (GCP) and International Council for Harmonization (ICH) guidelines.
- Ability to work independently and remotely.
protocol compliance,interpretation,clinical research,site management,clinical trial monitoring,reviewing essential study documents,clinical monitoring,regulatory compliance,case report forms,medical writing,ich guidelines,clinical trials,gcp,drug development process,clinical trial management systems (ctms),medical terminology,electronic data capture (edc) systems,data analysis
Employment Type
Full Time
Company Industry
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
